光激发
动力学(音乐)
材料科学
分子动力学
从头算
化学物理
从头算量子化学方法
自旋(空气动力学)
分子物理学
原子物理学
凝聚态物理
计算化学
激发态
物理
量子力学
热力学
化学
分子
声学
作者
Linjie Chen,Zhenfa Zheng,Qijing Zheng,Qunxiang Li,Jin Zhao
标识
DOI:10.1007/s40843-023-2838-5
摘要
Using photoexcitation to manipulate the magnetic moment in two-dimensional (2D) materials paves the way for the design of opto-spintronic devices. In this work, using ab initio nonadiabatic molecular dynamics simulation, we studied how photoexcitation changed the magnetic moment in the 2D ferromagnetic metal VSe2. The spin-orbit coupling and phonon excitation lead to the loss of the original spin orientation in both the spin-up and spin-down orbitals, forming a spin-mixing region approximately 1.0 eV above the Fermi level. When spin-up or spin-down electrons pass through this region during relaxation, they lose their original spin orientation. However, spin-down electrons relax approximately an order of magnitude faster than spin-up electrons, as the relaxation for spin-down is primarily intraband, while spin-up electrons undergo interband relaxation. Such different dynamical behaviors for spin-up and spin-down electrons result in the magnetic moment of VSe2 initially rising within approximately 10 fs after optical excitation, corresponding to the loss of the original spin orientation for spin-down electrons. Subsequently, it decreases by approximately 100 fs, corresponding to the loss of spin orientation for spin-up electrons. Finally, the total magnetic moment of the system gradually recovers to the preexcitation level on the order of picoseconds. This work provides new insight into how photoexcitation controls the magnetic properties of 2D materials.
科研通智能强力驱动
Strongly Powered by AbleSci AI